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52884-09-0

(2SR,3RS)-3-methyl-2-phenylpent-4-yn-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 52884-09-0 Structure

  • Basic information

    1. Product Name: (2SR,3RS)-3-methyl-2-phenylpent-4-yn-2-ol
    2. Synonyms:
    3. CAS NO:52884-09-0
    4. Molecular Formula:
    5. Molecular Weight: 174.243
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52884-09-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (2SR,3RS)-3-methyl-2-phenylpent-4-yn-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2SR,3RS)-3-methyl-2-phenylpent-4-yn-2-ol(52884-09-0)
    11. EPA Substance Registry System: (2SR,3RS)-3-methyl-2-phenylpent-4-yn-2-ol(52884-09-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 52884-09-0(Hazardous Substances Data)

52884-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52884-09-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,8 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 52884-09:
(7*5)+(6*2)+(5*8)+(4*8)+(3*4)+(2*0)+(1*9)=140
140 % 10 = 0
So 52884-09-0 is a valid CAS Registry Number.

52884-09-0Relevant articles and documents

Asymmetric propargylation of ketones using allenylboronates catalyzed by chiral biphenols

Barnett, David S.,Schaus, Scott E.

supporting information; experimental part, p. 4020 - 4023 (2011/10/02)

Chiral biphenols catalyze the enantioselective asymmetric propargylation of ketones using allenylboronates. The reaction uses 10 mol % of 3,3′-Br2-BINOL as the catalyst and allenyldioxoborolane as the nucleophile, in the absence of solvent, and

Preparation of syn -Tertiary homoallylic alcohols utilizing allenyltitanocenes generated by reductive titanation of γ- Trimethylsilylpropargylic carbonates

Yatsumonji, Yasutaka,Sugita, Takenori,Tsubouchi, Akira,Takeda, Takeshi

supporting information; experimental part, p. 1968 - 1971 (2010/07/06)

Figure presented syn-Tertiary homoallylic alcohols were obtained by the reaction of α-silylallenyltitanocenes generated by the reductive titanation of γ-silylpropargylic carbonates with Cp2Ti[P(OEt) 3]2 with ketones and fo

Preparation of organoaluminum reagents from propargylic bromides and aluminum activated by PbCl2and their regio- And diastereoselective addition to carbonyl derivatives

Guo, Li-Na,Gao, Hongjun,Mayer, Peter,Knochel, Paul

supporting information; experimental part, p. 9829 - 9834 (2010/11/02)

Various propargylic and allenic aluminum reagents have been easily prepared by a direct insertion of aluminum into propargylic bromides in the presence of PbCl2 (1 mol%). These organoaluminum reagents react with carbonyl compounds to afford the

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